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Choosing BeneFIXChoosing BeneFIXChoosing BeneFIXPersonalised dosing Product InformationProduct InformationEfficacy & SafetyAdministration & StorageSupport & ResourcesSupport & ResourcesMaterialsVideosOrdering BeneFIXContact Us

For BeneFIX® (nonacog alfa) Prescribing Information for Great Britain and Northern Ireland click here.

Personalised Dosing

BeneFIX® offers frequent, flexible dosing so you and your patients are covered for everyday life. Dose and dose intervals should be based on patients' bleeding profile.1

Dosing with BeneFIX

R2 Device

BeneFIX® powder and solvent for solution for injection is available in 250 IU, 500 IU, 1000 IU, 2000 IU.2

Calculate your patients required dose of BeneFIX® 

For a recovery of 0.8 IU/dL, the required dose is determined using the following formula1:

The calculation of the required dose of BeneFIX can be based on the finding that one unit of factor IX activity per Kg body weight is expected to increase the circulating level of factor IX, an average of 0.8 IU/dL (range from 0.4 to 1.4 IU/dL) in patients ≥ 12 years.1

For further information consult BeneFIX Summary of Product Characteristics.


 

This image shows the R2 device colour-coded packaging. Each colour corresponds to a different vial dose, making it easier to identify.

Explore More
Choosing BeneFIX

Find out more about choosing BeneFIX: why and the commitment Pfizer has towards Haemophilia care.

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Efficacy & Safety 

Access data on the clinical efficacy & safety of BeneFIX® for prophylaxis, on-demand treatment, and surgery.

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Contact us

Contact us for more information on BeneFIX® and download our FAQ for supply and stock related queries.

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References

BeneFIX® Summary of Product Characteristics. For Great Britain, available here. For Northern Ireland, available here.BeneFIX® Patient Information Leaflet
PP-BEN-GBR-0634. July 2023

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search 

for MHRA Yellow Card in Google Play or Apple App Store

 

Adverse events should also be reported to Pfizer Medical Information on 01304 616161

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